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T19884CI 21100；化合物 T19884CI21100|||CI-21100；CI21100|||CI-21100
CI 21100 A kind of organic pigment, yellow powder. Heating at 150 ℃ for 20min slightly green. In concentrated sulfuric acid for the red light color, diluted brown light red; in concentrated nitric acid for the brown light yellow. Mainly used for coloring rubber, plastic products, etc., also used in ink and paint industry.
价 格：￥电议型 号：T19884产 地：中国大陆
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T1987PFI-2；化合物PFI-2PFI2|||PFI 2|||(R)-PFI-2；PFI2|||PFI 2|||(R)-PFI-2
PFI-2 is an effective, specific and cell-active lysine methyltransferase SETD7 inhibitor (Ki/IC50: 0.33/2 nM), 1000-fold selectivity over other methyltransferases and other non-epigenetic targets.
价 格：￥电议型 号：T1987产 地：中国大陆
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T19685Faldaprevir；化合物 T19685BI-201335|||BI201335|||BI 201335；BI-201335|||BI201335|||BI 201335
Faldaprevir is an effective NS3/NS4A protease inhibitor potentially for the treatment of HCV infection. Faldaprevir is known to inhibit P-glycoprotein, CYP3A4, and UDP-glucuronosyltransferase 1A1.
价 格：￥电议型 号：T19685产 地：中国大陆
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T15238Epoprostenol sodium；化合物 T15238Prostaglandin I2 sodium salt|||Prostacyclin sodium salt|||Flolan；Prost
Epoprostenol sodium is a potent inhibitor of platelet aggregation used in pulmonary hypertension and transplantation.
价 格：￥电议型 号：T15238产 地：中国大陆
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T11689ITI-214；化合物ITI214ITI214；ITI214
ITI-214 is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters, and ion channels, exhibits potent PDE1 inhibitory activity (Ki = 58 pM).
价 格：￥电议型 号：T11689产 地：中国大陆
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T11688ITI-214 free base；化合物 T11688ITI214 free base；ITI214 free base
ITI-214 free base is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters, and ion channels, exhibits potent PDE1 inhibitory activity (Ki = 58 pM).
价 格：￥电议型 号：T11688产 地：中国大陆
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T11594I2906；化合物 T11594I2906
I2906 showed antimycobacterial and cytotoxic activity against mycobacterium tuberculosis.
价 格：￥电议型 号：T11594产 地：中国大陆
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T11397GGTI298；化合物 T11397GGTI298
GGTI298, a CAAZ peptidomimetic and potent geranylgeranyltransferase I (GGTase I) inhibitor, efficiently blocks the processing of geranylgeranylated Rap1A while exerting minimal impact on the processing of farnesylated Ha-Ras. The inhibitor displays in vivo IC50 values of 3 μM for Rap1A and >20 μM for Ha-Ras, respectively.
价 格：￥电议型 号：T11397产 地：中国大陆
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T10701(+)-CBI-CDPI2；化合物 T10701(+)-CBI-CDPI2
(+)-CBI-CDPI2 is an enhanced functional analog of CC-1065.
价 格：￥电议型 号：T10701产 地：中国大陆
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T10673Carbacyclin；化合物 T10673Carbaprostacyclin|||Carba-PGI2；Carbaprostacyclin|||Carba-PGI2
Carbacyclin, a PGI2 analog, is a prostacyclin (PGI2) receptor agonist and vasodilator with potent inhibitory platelet aggregation.
价 格：￥电议型 号：T10673产 地：中国大陆
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T0431Abexinostat；阿贝司他CRA 24781|||PCI24781|||PCI-24781|||PCI 24781|||CRA 024781；CRA 24781|||阿贝司他|||PCI2478
PCI-24781 (Abexinostat (PCI24781)) is a new pan-HDAC inhibitor mainly targeting HDAC1 (Ki: 7 nM), also have moderate inhibitory for HDACs 2, 3, 6, and 10 and greater than 40-fold selectivity against HDAC8. Phase 1/2.
价 格：￥电议型 号：T0431产 地：中国大陆
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T0162Quetiapine；喹硫平ICI204636|||Quetiapin；ICI204636|||Quetiapin|||喹硫平
Quetiapine (ICI204636) is used for the therapy of schizophrenia, and for the treatment of acute manic episodes associated with bipolar I disorder. The mechanism of quetiapine´ action is thought by mediated through antagonist activity at serotonin and dopamine receptors. Specifically, the D1 and D2 dopamine, the α1 adrenoreceptor and α2 adrenoreceptor, and 5-HT1A and 5-HT2 serotonin receptor subtypes are antagonized. Quetiapine also can inhibit the histamine H1 receptor.
价 格：￥电议型 号：T0162产 地：中国大陆
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Fr13138Jedi2；化合物 Jedi2Jedi2
Jedi2 is a Piezo1 activator rather than a specific Piezo2 activator. Jedi2 binds to the mouse Piezo1 proteins with a K d of 2770 μM [1].
价 格：￥电议型 号：Fr13138产 地：中国大陆
